Toward a methodology for evaluating DNA variants in nuclear families

por Miller, Dustin B., Robison, Reid, Piccolo, Stephen R.
Publicado 2021

Real-world depression, anxiety and safety outcomes of intramuscular ketamine treatment: a retrospective descriptive cohort study

por Ahuja, Sachin, Brendle, Madeline, Smart, Leo, Moore, Claire, Thielking, Paul, Robison, Reid
Publicado 2022

Case report: Intramuscular ketamine or intranasal esketamine as a treatment in four patients with major depressive disorder and comorbid anorexia nervosa

por Keeler, Johanna Louise, Treasure, Janet, Himmerich, Hubertus, Brendle, Madeline, Moore, Claire, Robison, Reid
Publicado 2023

Breathwork Interventions for Adults with Clinically Diagnosed Anxiety Disorders: A Scoping Review

por Banushi, Blerida, Brendle, Madeline, Ragnhildstveit, Anya, Murphy, Tara, Moore, Claire, Egberts, Johannes, Robison, Reid
Publicado 2023

A case series of group-based ketamine-assisted psychotherapy for patients in residential treatment for eating disorders with comorbid depression and anxiety disorders

por Robison, Reid, Lafrance, Adele, Brendle, Madeline, Smith, Michelle, Moore, Claire, Ahuja, Sachin, Richards, Scott, Hawkins, Nicole, Strahan, Erin
Publicado 2022

Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine

por Fang, Han, Wu, Yiyang, Yang, Hui, Yoon, Margaret, Jiménez-Barrón, Laura T., Mittelman, David, Robison, Reid, Wang, Kai, Lyon, Gholson J.
Publicado 2017

KBG syndrome involving a single-nucleotide duplication in ANKRD11

por Kleyner, Robert, Malcolmson, Janet, Tegay, David, Ward, Kenneth, Maughan, Annette, Maughan, Glenn, Nelson, Lesa, Wang, Kai, Robison, Reid, Lyon, Gholson J.
Publicado 2016

Ketamine as a Novel Psychopharmacotherapy for Eating Disorders: Evidence and Future Directions

por Ragnhildstveit, Anya, Slayton, Matthew, Jackson, Laura Kate, Brendle, Madeline, Ahuja, Sachin, Holle, Willis, Moore, Claire, Sollars, Kellie, Seli, Paul, Robison, Reid
Publicado 2022

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

por Cannon, Dale S, Miller, Judith S, Robison, Reid J, Villalobos, Michele E, Wahmhoff, Natalie K, Allen-Brady, Kristina, McMahon, William M, Coon, Hilary
Publicado 2010

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

por Coon, Hilary, Villalobos, Michele E, Robison, Reid J, Camp, Nicola J, Cannon, Dale S, Allen-Brady, Kristina, Miller, Judith S, McMahon, William M
Publicado 2010

Integrating precision medicine in the study and clinical treatment of a severely mentally ill person

por O’Rawe, Jason A., Fang, Han, Rynearson, Shawn, Robison, Reid, Kiruluta, Edward S., Higgins, Gerald, Eilbeck, Karen, Reese, Martin G., Lyon, Gholson J.
Publicado 2013

SCN8A mutation in a child presenting with seizures and developmental delays

por Malcolmson, Janet, Kleyner, Robert, Tegay, David, Adams, Whit, Ward, Kenneth, Coppinger, Justine, Nelson, Lesa, Meisler, Miriam H., Wang, Kai, Robison, Reid, Lyon, Gholson J.
Publicado 2016

Cannabis-assisted psychotherapy for complex dissociative posttraumatic stress disorder: A case report

por Ragnhildstveit, Anya, Kaiyo, Miriam, Snyder, Matthew Brian, Jackson, Laura Kate, Lopez, Alex, Mayo, Chasity, Miranda, Alyssa Claire, August, River Jude, Seli, Paul, Robison, Reid, Averill, Lynnette Astrid
Publicado 2023

SeqHBase: a big data toolset for family based sequencing data analysis

por He, Min, Person, Thomas N, Hebbring, Scott J, Heinzen, Ethan, Ye, Zhan, Schrodi, Steven J, McPherson, Elizabeth W, Lin, Simon M, Peissig, Peggy L, Brilliant, Murray H, O'Rawe, Jason, Robison, Reid J, Lyon, Gholson J, Wang, Kai
Publicado 2015

Massively parallel sequencing identifies a previously unrecognized X-linked disorder resulting in lethality in male infants owing to amino-terminal acetyltransferase deficiency

por Rope, Alan F, Wang, Kai, Evjenth, Rune, Xing, Jinchuan, Johnston, Jennifer J, Swensen, Jeffrey J, Johnson, W Evan, Moore, Barry, Huff, Chad D, Bird, Lynne M, Carey, John C, Opitz, John M, Stevens, Cathy A, Schank, Christa, Fain, Heidi Deborah, Robison, Reid, Dalley, Brian, Chin, Steven, South, Sarah T, Pysher, Theodore J, Jorde, Lynn B, Hakonarson, Hakon, Lillehaug, Johan R, Biesecker, Leslie G, Yandell, Mark, Arnesen, Thomas, Lyon, Gholson J
Publicado 2011

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

por O’Rawe, Jason A., Wu, Yiyang, Dörfel, Max J., Rope, Alan F., Au, P.Y. Billie, Parboosingh, Jillian S., Moon, Sungjin, Kousi, Maria, Kosma, Konstantina, Smith, Christopher S., Tzetis, Maria, Schuette, Jane L., Hufnagel, Robert B., Prada, Carlos E., Martinez, Francisco, Orellana, Carmen, Crain, Jonathan, Caro-Llopis, Alfonso, Oltra, Silvestre, Monfort, Sandra, Jiménez-Barrón, Laura T., Swensen, Jeffrey, Ellingwood, Sara, Smith, Rosemarie, Fang, Han, Ospina, Sandra, Stegmann, Sander, Den Hollander, Nicolette, Mittelman, David, Highnam, Gareth, Robison, Reid, Yang, Edward, Faivre, Laurence, Roubertie, Agathe, Rivière, Jean-Baptiste, Monaghan, Kristin G., Wang, Kai, Davis, Erica E., Katsanis, Nicholas, Kalscheuer, Vera M., Wang, Edith H., Metcalfe, Kay, Kleefstra, Tjitske, Innes, A. Micheil, Kitsiou-Tzeli, Sophia, Rosello, Monica, Keegan, Catherine E., Lyon, Gholson J.
Publicado 2015